Apparatus for analyzing a volatile composition of matter releasably bonded to a pliable porous substrate and process for using said apparatus

ABSTRACT

Described is apparatus and a process for analyzing a volatile composition such as a perfume composition located on the surface and/or in the interstices of a planar pliable porous substrate such as a towel section. A planar surface of the substrate which contains the volatile composition is initially juxtaposed adjacent a solid wall (e.g., glass frit) porous to a nonreactive carrier gas such as air, nitrogen or carbon dioxide, and fully and tightly covers the porous section of the wall. The carrier gas is passed through the porous section of the wall and then through the pliable porous substrate section which is adjacent to the wall; after which the carrier gas contains molecules of each component of the volatile composition. The composition-carrier gas mixture is then passed through a trapping substance (e.g., TENAX®) which entraps the molecules of each component of the volatile composition. The volatile composition is then analyzed (e.g., using GLC and NMR techniques) after removing the trapping substance containing the entrapped molecules from the apparatus.  
     In a second embodiment of the invention the planar porous substrate is rotated and the movement of the fragrance from the substrate is measured.

RELATED APPLICATION

[0001] This application is a continuation-in-part of my application filed on Jun. 18, 1999, U.S. Ser. No. 09/336,055, the contents of which are hereby incorporated by reference as if set forth in its entirety.

BACKGROUND OF THE INVENTION

[0002] My invention covers apparatus for analyzing a volatile composition of matter which is releasably bonded to a pliable porous substrate such as a towel, as well as a process for using such apparatus.

[0003] The properties of a pliable substrate (including physical, chemical and microbiological properties) affect the behavior of the substrate with respect to chemicals, particularly volatile chemicals, either naturally present in or on the substrate in a substance applied thereto and so affect the chemicals present in a headspace above the substrate. Conversely, the chemicals entrapped in the interstices of a porous substrate or on the surface of the porous substrate have an effect upon the properties of the substrate, for example, if the substrate is a towel and the towel contains a fragrance, the concentration of that fragrance and the nature of the fragrance in the particular substrate will affect the ultimate aroma in the headspace above the substrate after the substrate is utilized, washed and dried.

[0004] Considerably complicated techniques exist in the prior art for analysis of volatile materials contained within a substrate. Thus, U.S. Pat. No. 5,891,729 issued on Apr. 6, 1999 (“METHOD FOR SUBSTRATE CLASSIFICATION”) discloses a substrate (e.g., skin of unknown type, fabric or hard surfaces) as being characterized by analyzing chemicals emanating from the substrate or from a substance (e.g., a test formulation comprising a mixture of volatile chemicals) applied to the substrate. U.S. Pat. No. 5,891,729 indicates that analysis is preferably done using a volatile chemicals sensor, desirably a sensor comprising an array of conducting polymer sensors. The chemical analysis data obtained in this way, according to U.S. Pat. No. 5,891,729, may be statistically analyzed, e.g., by Euclidean distance mapping or principal component analysis for ease of handling. It is further indicated in U.S. Pat. No. 5,891,729 that having characterized a surface in this manner, products, e.g., cosmetic and cleaning products, may be formulated for optimized performance on that substrate. More specifically, U.S. Pat. No. 5,891,729 discloses a method of characterizing a substrate which comprises applying a test formulation to said substrate, subsequently collecting volatile chemicals in a headspace above the substrate, determining a profile of the volatile chemicals so emanated and using said profile to characterize the substrate. Specific examples of substrates in U.S. Pat. No. 5,891,729 are skin, wood, hair, clothing, carpets, plastics, surfaces, ceramic tiles, wool, fabric or perfumed products.

[0005] Noting the complexity of the methods and techniques of U.S. Pat. No. 5,891,729, it is apparent that a need exists for a more standardized and simplified technique for analysis of a volatile composition of matter releasably bonded to a pliable porous substrate such as a towel.

[0006] Thus, for example, U.S. Pat. No. 5,891,835 issued on Apr. 6, 1999 discloses a cleaner impregnated towel comprising a flexible porous substrate and impregnated into the substrate a cleaner formulation comprising d-limonene, dibasic acid ester, N-methyl-2-pyrrolidone, secondary alcohol ethoxylate, sodium lauryl sulfate, polysorbate 80, a salt of a coconut oil, fatty acid ester of isethionic acid, glycerine, ethyl alcohol, an antimicrobial preservative and, optionally, water. Although the composition impregnated into the substrate is known initially, after the substrate is utilized, there is no teaching of the nature or concentration of the components impregnated into the substrate after initial use or after repeated use of the substrate, nor is there any teaching in U.S. Pat. No. 5,891,835 or 5,891,729 of apparatus or processes for analyzing the contents of such substrate quantitatively or qualitatively using a standardized, simplified procedure as is the case with the instant invention.

SUMMARY OF THE INVENTION

[0007] My invention is directed to apparatus which will permit determination of compounds and their concentrations in the headspace over dry cloth as well as moist cloth and other substrates. The compounds are releasably bonded to the surface and/or in the interstices of the porous substrate.

[0008] More specifically, my invention is directed to apparatus and a process for analyzing a volatile composition such as a perfumery composition located on the surface and/or in the interstices of a planar pliable porous substrate such as a towel section.

[0009] In practicing my invention, a planar surface of the substrate which contains the volatile composition is initially juxtaposed adjacent a solid wall (e.g., glass frit) porous to a nonreactive carrier gas such as air, nitrogen or carbon dioxide and fully and tightly covers the porous section of the wall. The carrier gas is passed through the porous section of the wall and then through the pliable porous substrate section which is adjacent the wall, after which the carrier gas will contain molecules of each component of the volatile composition. The composition-carrier gas mixture is then passed through a trapping substance (e.g., TENAX®) which entraps the molecules of each component of the volatile composition. The volatile composition is then analyzed (e.g., using GLC, NMR and mass spectral techniques) after removing the trapping substance containing the entrapped molecules from the apparatus.

[0010] Thus, my invention is directed to apparatus for quantitatively and qualitatively analyzing a volatile substance such as a perfumery material releasably bonded to a substantially planar pliable porous substrate having an inner surface and an outer surface. The substrate is porous to the passage of a carrier gas therethrough in a direction substantially perpendicular to the inner and outer surfaces of the planar pliable porous substrate. The apparatus comprises:

[0011] (a) hollow enclosure means (which can be cylindrically shaped or elliptical-cylindrically shaped) having:

[0012] (i) hollow outer enclosure means comprising a hollow outer enclosure means first void space, and surrounding said outer enclosure means first void space, an outer gas-impermeable enclosure means wall having exit port means therethrough and entirely surrounding inner enclosure means whereby a second void space exists having volume V₂ within said outer enclosure means and without said inner enclosure means; and

[0013] (ii) inner enclosure means located entirely within said outer enclosure means first void space comprising an inner enclosure means third void space, and having two spaced-apart oppositely situated end sections and a central section juxtaposed and communicating with each of said oppositely-situated end sections, said central section consisting essentially of support means having a substantially gas-permeable outer geometric laminar surface with at least one laminar gas-permeable section for both (a) supporting the pliable porous substrate whereby, when the apparatus is in use, said porous substrate covers said laminar permeable section of said central section in an all-encompassing manner; and (b) enabling carrier gas to flow from within said inner enclosure means third void space to the second void space within said outer enclosure and without said inner enclosure, in a direction substantially perpendicular to and through said porous substrate, each of the two end sections being impervious to the flow of gas therethrough and one of said end sections having an entry port means communicating from without said hollow outer enclosure means to the first void space within said inner enclosure means, said first void space having a volume V₁;

[0014] (b) analytical apparatus means located downstream from said hollow enclosure means and communicating with the exit port means thereof, comprising tube trapping means whereby volatile substance molecules emitted from said pliable porous substrate during gas flow therethrough (for example, perfume molecules such as phenyl ethyl alcohol molecules emitted from a towel section) are entrapped in said tube trapping means; and

[0015] (c) upstream from said hollow enclosure means or downstream from said analytical apparatus means, inert gas flow effecting means for effecting the flow of inert gas sequentially (i) through said entry port means; (ii) through porous pliable substrate means located on said support means; (iii) through said exit port means; and (iv) through said analytical apparatus means.

[0016] My invention is also directed to a process for quantitatively and qualitatively analyzing a volatile substance (such as a fragrance composition or an insect-repelling composition) releasably bonded to a substantially planar pliable porous substrate (for example, a cloth or a towel fabricated from cotton or polyester) having an inner surface and an outer surface comprising the step of:

[0017] (a) providing the apparatus as set forth, supra;

[0018] (b) providing a substantially planar pliable porous substrate having releasably bonded thereto a volatile substance such as a perfumery substance;

[0019] (c) juxtaposing in an all-encompassing manner said porous substrate with said support means of said central section of said inner enclosure means of said apparatus whereby the inner surface of said porous substrate is removably adhered to and intimately adjacent to the entirety of the laminar gas-permeable section of the outer geometric laminar surface of the support means;

[0020] (d) effecting the flow of carrier gas sequentially (i) from a location upstream from the entry port means; (ii) into the inner enclosure means through said entry port means; (iii) past said support mean; (iv) through said porous substrate means in a direction substantially perpendicular thereto, in a substantially evenly distributed manner across the inner and outer surface thereof; (v) into and through said second void space; (vi) through said exit port means of said hollow outer enclosure means and into and through said analytical apparatus means; and (vii) whereby volatile substance molecules (e.g., perfumery composition molecules) emitted from said porous substrate are trapped in a trapping means of the analytical apparatus means; and

[0021] (e) employing the analytical apparatus means whereby analysis of the releasably bonded volatile molecules is effected.

[0022] Another embodiment of the present invention provides for the rotation of the pliable porous substrate thereby releasing a volatile composition of matter from the substrate. More specifically, the present invention provides for both methods and apparatus for carrying out this embodiment.

[0023] The invention comprises apparatus for quantitatively and qualitatively analyzing a volatile substance releasably bonded to a substantially planar pliable porous substrate having an inner surface and an outer surface, said substrate being porous to the passage of a carrier gas comprising:

[0024] (a) hollow enclosure means supported by a retaining means thereby creating a hollow enclosure void space and, having exit port means therethrough;

[0025] (b) analytical apparatus means located downstream from said hollow enclosure means and communicating with the exit port means thereof, comprising trapping means whereby volatile substance molecules emitted from said pliable porous substrate during gas flow therethrough are entrapped in said tube trapping means; and

[0026] (c) upstream from said hollow enclosure means or downstream from said analytical apparatus means, inert gas flow effecting means for effecting the flow of inert gas sequentially (I) through said entry port means; (II) through porous pliable substrate means located on said support means; (III) through said exit port means; and (IV) through said analytical apparatus means; and

[0027] (d) means for moving the retaining means; and

[0028] (e) means for attaching a porous pliable substrate means to the retaining means.

[0029] The method comprises the use of the apparatus described above as follows:

[0030] A process for quantitatively and qualitatively analyzing a volatile substance releasably bonded to a substantially planar pliable porous substrate having an inner surface and an outer surface comprising the steps of:

[0031] (a) providing the apparatus set forth hereinabove;

[0032] (b) providing said porous substrate;

[0033] (c) moving said porous substrate with said support means;

[0034] (d) effecting the flow of carrier gas sequentially (I) from a location upstream from the entry port means; (II) into the hollow enclosure means; (III) in proximity of said porous substrate means; (IV) through said exit port means of said hollow outer enclosure means and into and through said analytical apparatus means; and (V) whereby volatile substance molecules emitted from said porous substrate are trapped in said analytical apparatus means; and

[0035] (e) employing the analytical apparatus means whereby analysis of the volatile molecules is effected.

DETAILED DESCRIPTION OF THE INVENTION

[0036] Preferably, the hollow enclosure means of the above-described apparatus contains two concentric cylindrical enclosures, with the outer cylindrical enclosure being impervious to gas except for an exit port and with the inner enclosure means having an entry port and having a centrally located solid porous surface (e.g., glass frit, or solid microporous polymer).

[0037] Preferably, after the pliable porous substrate is in place on the inner enclosure, carrier gas is forced through the inner enclosure past the porous substrate into the outer enclosure and then out of the outer enclosure into the analytical means which preferably contains a trapping material. The carrier gas, such as nitrogen, air or carbon dioxide, is inert and nonreactive with the porous substrate or with the volatile substance releasably bonded to the porous substrate. The carrier gas can either be forced through from a pressurized device upstream from the hollow enclosure means (e.g., a pressurized carbon dioxide cylinder), or the carrier gas can be pulled through using means downstream from the analytical apparatus means such as a vacuum pump.

[0038] Whether the inert gas flow effecting means is upstream from the remainder of the apparatus or downstream from the remainder of the apparatus, it is preferable to have a gas filter in place in the apparatus of my invention, upstream from the hollow enclosure means so that the inert gas is free of any contaminants which would interfere with the analysis of the composition releasably bonded to the substantially planar pliable porous substrate (e.g., towel section).

[0039] Preferably, the hollow outer enclosure means of the hollow enclosure means part of the apparatus of my invention is cylindrical and has a height dimension of from about 4 cm up to about 20 cm and a diameter dimension of from about 4 cm up to about 12 cm. Preferably, the inner enclosure means of the hollow enclosure means part of the apparatus of my invention is cylindrical and has a height dimension between from about 50% up to about 85% of the height dimension of the hollow outer enclosure means and a diameter dimension of from about 40% up to about 70% of the diameter dimension of the hollow outer enclosure means.

[0040] The support means part of the inner enclosure means (that is, the central section of the inner enclosure means) is preferably cylindrical or substantially cylindrical in shape and as stated, supra, is preferably glass frit or microporous polymer. However, other suitable support means are useful in the practice of my invention, for example, the material which is marketed as cylindrical filter screens by the B.C. McDonald & Company of St. Louis, Mo. 63132 under the description of “Ronningen-Petter Woven Wire Screen”; or Ronningen-Petter Woven Synthetic Screen (illustrated in FIG. 1E which is described in the Brief Description of the Drawings and in the Detailed Description of the Drawings sections, infra); or the Ronningen-Petter Perforated Screen. The Ronningen-Petter Screens are manufactured by the Dover Corporation/Ronningen-Petter Division, P.O. Box 188, Portage, Mich. 49081. The Ronningen-Petter Cylindrical Screens useful as support means in the practice of our invention are specifically described in literature published by Ronningen-Petter entitled “how to select filter screens for the removal of trace contaminants in a closed liquid system.”

[0041] Other support means useful in fabrication of the central section of the inner enclosure means of the apparatus of my invention are described in U.S. Pat. No. 5,762,797 issued on Jun. 9, 1998 entitled “ANTIMICROBIAL FILTER CARTRIDGE,” the specification for which is incorporated by reference herein, and U.S. Pat. No. 5,868,933 issued on Feb. 9, 1999 entitled “ANTIMICROBIAL FILTER CARTRIDGE”, the specification for which is incorporated by reference herein.

[0042] With respect to the analytical apparatus means located downstream from the hollow enclosure means and communicating with the exit port means of the hollow outer enclosure means, the analytical means part of the apparatus of my invention as stated, supra, comprises tube trapping means whereby volatile substance molecules emitted from the pliable porous substrate during gas flow therethrough are entrapped in the tube trapping means. The tube trapping means preferably consists of a tube having a length in the range of from about 2 cm up to about 4 cm and a diameter of from about 0.1 cm up to about 0.4 cm. Thus, various trapping materials are useful in the practice of my invention. As stated, supra, TENAX® is a preferable material. Various forms of TENAX® are useful, for example, TENAX®-GC. TENAX® is a registered trademark of ENKA, N.V. of the Kingdom of the Netherlands (CAS Registration No. 2438-68-9). Other forms of TENAX® and methods of production of such forms of TENAX® are described in the following U.S. patents, the disclosures of which are incorporated by reference herein:

[0043] U.S. Pat. No. 3,400,100 issued on Sep. 30, 1968 (“PROCESS FOR THE PREPARATION OF POLYPHENYLENE ETHERS”);

[0044] U.S. Pat. No. 3,644,227 issued on Feb. 22, 1972 (“SEPARATION OF POLY(2-6-DIMETHYL-1,4-PHENYLEOXIDE”) FROM ITS BLENDS WITH OTHER POLYMERS);

[0045] U.S. Pat. No. 3,703,564 issued on Nov. 21, 1972 (BIS-POLYPHENYLENEOXIDE]ESTER BLOCK COPOLYMERS”);

[0046] U.S. Pat. No. 4,431,779 issued on Feb. 14, 1984 (POLYETHERAMIDE-POLYPHENYLENE ETHER BLENDS”); and

[0047] U.S. Pat. No. 4,801,645 issued on Jan. 31, 1989 (“THERMOPLASTIC RESIN COMPOSITION”).

[0048] TENAX®-GC is actually a polyphenyleneoxide defined according to the structure:

[0049] wherein N is an integer of from about 100 up to about 150.

[0050] Other trapping materials useful in the practice of my invention are as follows:

[0051] Activated Carbon marketed by Aldrich Chemical Company of 1001 West Saint Paul Avenue, Milwaukee, Wis. 53233 (Catalog Nos. 16, 155-1; 29, 259-1; 24, 223-3; 24, 224-1; and 24, 227-6);

[0052] Activated Alumina marketed by Sigma Chemical Company of St. Louis, Mo. (Catalog Nos. A8753; A8878; A9003; A1522; and A2272);

[0053] Silica Gels marketed by Sigma Chemical Company (for example, Catalog Nos. S4004; S6628; and H8506); and

[0054] CHROMOSORB® (registered trademark of the Johns-Manville Company of Manville, N.J.), such as CHROMOSORB® LC-2; CHROMOSORB® LC-3; AND CHROMOSORB® LC-7, marketed by Sigma Chemical Company under Catalog Nos. C 0641; C 0766; C 5517 and C 6269.

[0055] The analytical apparatus means useful in the practice of my invention may contain, in place of the TENAX® trapping substance, solid phase microextraction materials (“SPME” materials) such as those described in Bulletin 869 published by SUPELCO, INC., Supelco Park, Bellefonte, Pa. 16823-0048. An SPME example useful in the practice of my invention is 100 μm polydimethylsiloxane fiber, Catalog No. 5-7300 of Supelco, Inc. The Supelco, Inc. Bulletin 869 is incorporated by reference herein. An additional description of the SPME (solid phase microextraction) technique useful in conjunction with the practice of my invention is the paper, Elmore, et al, J. Agric. Food Chem., 1997, Volume 45, pages 2638-2641, entitled “Comparison of Dynamic Headspace Concentration on Tenax [TENAX®] with Solid Phase Microextraction for the Analysis of Aroma Volatiles,” incorporated by reference herein.

[0056] As stated, supra, the means for effecting the flow of inert gas sequentially (i) through the entry port means of the inner enclosure means; (ii) and through the porous pliable substrate means located on the support means of the apparatus of my invention can be located downstream from the analytical apparatus means. If that is the case, the inert gas flow effecting means is a negative pressure pump means, preferably a vacuum pump of the “low flow” variety, for example, “Low Flow” pumps marketed by the Ametek Company of Largo, Fla. 34643 (the “Ametek Constant flow Sampler”).

[0057] The flow rate of inert carrier gas past the porous pliable substrate is preferably at a rate in the range of from about 20 ml per minute up to about 200 ml per minute of carrier gas, e.g., nitrogen, air or carbon dioxide.

[0058] At the indicated rates of carrier gas flow, a range of molar rates of release of volatile composition will occur from the porous substrate, e.g., towel section, in accordance with the following algorithm: ${\Delta \quad n} = {n_{1}\left\lbrack {{\frac{V_{1}}{V_{2}}^{- {\frac{2C_{V}}{zR}{\lbrack\frac{T_{2} - T_{1}}{T_{2} + T_{1}}\rbrack}}}} - 1} \right\rbrack}$

[0059] wherein

[0060] n₁ is the carrier gas flow rate in gram moles per hour;

[0061] Δn is the molar flow rate (in gram moles per hour) of release of volatile composition from the pliable porous substrate;

[0062] V₁ is the volume of the inner enclosure;

[0063] T₁ is the temperature of the void space of the inner enclosure in °K (degrees Kelvin);

[0064] V₂ is the volume between the porous pliable substrate and the outer enclosure;

[0065] T₂ is the temperature of the carrier gas and volatile composition released from the pliable porous substrate (that is, the temperature of volume V₂) in °K;

[0066] R is the gas constant $\left\lbrack {0.08206\quad \frac{{liter} - {atm}}{{{gm}\quad {mole}} - {{^\circ}\quad {K.}}}} \right\rbrack;$

[0067] Z is the compressibility factor of the carrier gas; and

[0068] C_(v) is the heat capacity of the carrier gas defined as $\left( \frac{\partial E}{\partial T} \right)_{V},$

[0069] wherein

[0070] E is the internal energy of the carrier gas during flow through the apparatus of my invention.

[0071] In another embodiment of the present invention, the pliable porous substrate is put into motion, preferably rotated, most preferably rotated at a controlled rate to simulate the ability of a fragrance to be released from the substrate when the substrate is moved. For example, this movement is intended to simulate the release of a fragrance from a sheet when the sheet is being placed upon a bed.

[0072] When the substrate is rotated it is desirable to provide a gentle, but thorough movement of the substrate. The movement can be done in various directions, such as a back and forth motion, an elliptical motion or most preferably in a circular motion. The circular motion is most preferred in that the rotation of the substrate on a rotating shaft is easily accomplished as well as providing a seal between the rotating shaft and enclosure means. The enclosure means could be enlarged such that all equipment is enclosed within the enclosure means; however, that makes analysis of the volatile compounds that are removed from the substrate more difficult.

[0073] Preferably, the rotating shaft is controlled via a motor means such as an electric motor, preferably by a variable control source. The rotation of the shaft should be from about 10 to about 150 revolutions per minute, typically from about 30 to about 120 and preferably from 50 to about 90 revolutions per minute. In a highly preferred embodiment, the rotation of the substrate should be about 82 revolutions per minute. This rpm is sufficient to simulate the movement of the substrate in routine motion without being unduly harsh, thereby removing too much of the fragrance, or too gently which might not release sufficient fragrance from the substrate.

[0074] The carrier gas, preferably an inert gas, is provided at a rate of from 0.1 to about 1.0 liter/minute, typically from about 0.2 to about 0.8 and preferably from about 0.3 to about 0.7 liter/minute. The most preferred flowrate is about 0.5 liter/minute.

[0075] The analysis of the headspace is carried out in the same manner as described hereinabove. The analysis means monitors the headspace of the enclosure means on a substantially continues manner. The contents of the headspace is then carried onto the trapping materials and the analysis is conducted as described herein above.

BRIEF DESCRIPTION OF THE DRAWINGS

[0076]FIG. 1A is a schematic block flow diagram showing the operation of the apparatus of my invention and the process of my invention.

[0077]FIG. 1B is another schematic block flow diagram showing the operation of the apparatus of my invention as well as the process of my invention and showing the use of pressure measuring devices in conjunction with the apparatus of my invention; and, in addition, showing the use of inert gas flow effecting means for effecting the flow of inert gas through the apparatus of my invention, upstream from the hollow enclosure portion of the apparatus of my invention, specifically as a pressurized gas source (e.g., cylinder of pressurized air).

[0078]FIG. 1C is another schematic block flow diagram showing the operation of the apparatus of my invention and the process of my invention and also showing inert gas flow effecting means for effecting the flow of inert gas through the apparatus of my invention, which flow effecting means is in the form of vacuum pump means downstream from the analytical apparatus means.

[0079]FIG. 1D is another schematic block flow diagram showing the use of the apparatus of my invention when in actual operation analyzing a pliable porous substrate material containing material to be analyzed (e.g., a fragrance composition).

[0080]FIG. 1E is a cutaway perspective diagram of an example of a laminar gas-permeable section of the central section of the inner enclosure means of the apparatus of my invention (“Ronningen-Petter Woven Synthetic Screen” manufactured by the Ronningen-Petter Division of the Dover Corporation, P.O. Box 188, Portage, Mich. 49081).

[0081]FIG. 2 is a detailed cutaway side elevation view of a preferred embodiment of the apparatus of my invention showing the employment of fritted glass as a laminar gas permeable section of the central section of the inner enclosure means of the apparatus of my invention.

[0082]FIG. 3A is a perspective view of a preferred embodiment of the apparatus of my invention, showing the outer enclosure means fabricated from ceramic quartz glass and showing the central part of the inner enclosure means fabricated from fritted glass.

[0083]FIG. 3B is a perspective view of a preferred embodiment of that part of the apparatus of my invention which is the inner enclosure means wherein the central section consists of a fritted glass laminar gas-permeable section and wherein the porous pliable planar substrate to be analyzed is a towel section about to be placed fully covering and adjacent to the fritted glass section of the inner enclosure means.

[0084]FIG. 3C is a top cutaway schematic view of the inner enclosure means of the apparatus of my invention having juxtaposed and adjacent thereto the porous pliable substrate to be analyzed for a volatile composition contained thereon or in the interstices thereof.

[0085]FIG. 4 is the GC-mass spectrum of a fragrance composition releasably bonded to a towel section, which composition was analyzed for using the apparatus and process of my invention according to the procedure of Example I, infra (conditions: 50 meter×320μ×0.52μ bonded fused silica methyl silicone column programmed from 80-220° C. at 8° C. per minute).

[0086]FIG. 5 is a block schematic block flow diagram showing the operation of the apparatus and the process of my invention, wherein the porous pliable substrate is rotated about a shaft.

[0087]FIGS. 6A and 6B are chromatograms of a fragrance, measured while the pliable substrate is stationary and retested while it is in motion.

[0088]FIG. 7 is the graphical representation of the amount of fragrance detected by the apparatus of the present invention as tested at rest and also while in motion.

DETAILED DESCRIPTION OF THE DRAWINGS

[0089] Referring to FIGS. 1A, 1B, 1C and 1D, gas from gas source 10 is passed through line 12 past valve 14 through carrier gas filter 16 (optionally) through line 17 into the inner enclosure means 19, which is a support means for porous material 20. The carrier gas passes through entry port 40 into void 34. The inner enclosure means has top 37 and base 36. The inner enclosure means is supported via support 35 within the outer enclosure means 18. Carrier gas flows from void 34 into void 25 of the outer enclosure means (with the flow being shown by reference numeral 26). The carrier gas is then passed through line 21 past valve 31 into and through trapping means 22 wherein molecules of volatile material from the porous material at 20 are trapped. The trapping substance containing trapped molecules is then conveyed via route 28 to analysis means 24 (e.g., NMR, IR and mass spectral analytical equipment). Overall, the apparatus is indicated by reference numeral 100.

[0090] Specifically referring to FIG. 1B, pressurized gas (e.g., air) from, for example, a pressurized air vessel 11, is passed through line 12 into the apparatus of my invention, initially through line 17 via entry port 40. In FIG. 1B, pressure indicator 13 is located on line 12, and pressure indicator 27 is located in the outer enclosure means 18 whereby a pressure drop between line 14 primarily across porous wall 20 is measured.

[0091] Referring specifically to FIG. 1C, carrier gas from gas source 10 is pulled through the apparatus by means of vacuum pump means 23 located downstream from the trapping means 22. Inert carrier gas is pulled through the apparatus using vacuum pump means 23 through line 28 which is connected to trapping means 22. The resulting trapped molecules are then conveyed on the trapping substance via conveying means 30 to analysis means 24.

[0092] Referring specifically to FIG. 1D, the central section of inner enclosure means 19 is composed of glass frit shown by reference numeral 42. Carrier gas entering at entry port 40 into void 34 within the inner enclosure means then passes through the glass frit 42 and through the pliable porous substrate 20. The passage of the inert gas again is shown by reference numeral 26 wherein the carrier gas now containing molecules of volatile substance is passed into void 25 of outer enclosure means 18.

[0093] Referring to FIG. 1E, inner support means 42 a (Ronningen-Petter Woven Synthetic Screen) supports the pliable porous substrate containing volatile composition therein and/or thereon 20.

[0094] Referring to FIG. 2, inert carrier gas, e.g., air, passes through tube 17 past apparatus entry location 50 through entry port 40 (the entry port for the inner enclosure means) into void 34 and then through fritted glass 42 into the void between the outer container means 18 and the inner container means 19. The flow of carrier gas is shown by reference numeral 26. The top of the outer enclosure means is sealed to the lower section thereof 18 (which has base 18 a) with Teflon seal 49. The carrier gas containing molecules of volatile substance is then passed through line 21 past Swageloc connector 48 into TENAX® trap 22. The fritted glass support 42, in the case of the apparatus of FIG. 2, is 4″ in length×1.5″ in diameter and will hold a piece of cloth 4″ in length×5.25″ in width.

[0095] Referring to FIG. 3A, the apparatus 100 contains the upper inlet tube 18 and an inner enclosure means 42 having base 36 and outer enclosure means 18 having base 18 a. Carrier gas flows through tube 21 into TENAX® trap or SPME trap 22.

[0096] Referring to FIG. 3B, the pliable porous substrate 20 is a section of a towel which is to be juxtaposed immediately adjacent to and fully covering the fritted glass central part of the inner enclosure means 42.

[0097] Referring to FIG. 3C, the void space of the inner enclosure means 34 has carrier gas flowing therethrough in a direction perpendicular to the support means 42 for the pliable porous substrate 20 containing volatile composition (e.g., perfume composition) to be analyzed with the carrier gas flow being shown by reference numeral 26.

[0098] Referring to FIG. 5, a variable speed control means 100 is provided to a motor means 101 which is connected to a shaft 102 and sealing means 103. The sealing means is any suitable mechanical seal or packing which renders the hollow enclosure means substantially air tight, meaning that the contents of the hollow enclosure means will not leak into the ambient air, but rather will pass through the trap means 142 and the analysis means 143. The shaft means is connected with the retaining means 106 and the attachment means 105 which maintains the porous, pliable substrate 104 in place. Pins, clips, wire, tape, hook and loop fasteners as well as other fasteners can be employed to attach the substrate to the retaining means. The retaining means is preferable a wire or metal device larger than the substrate use to hold the substrate in place while it is being rotated.

[0099] The inert gas source 110 is provided through a line 128 preferably through a valve 113, also preferably through a filter 116, into the hollow enclosure means 118 through the inlet means. The carrier gas is preferably directed against the rotating porous substrate in a head-on or direct manner. This will remove more of the volatile organic components from the porous substrate. The carrier gas and the volatile organic material will then flow via the pressure differential through the trap 142 and the analysis means 143 as discussed hereinabove. Vacuum means 144 is preferably provided to create a low pressure area further enabling the movement of the carrier gas and volatile organic materials into the trap and analysis means. The hollow enclosure means is supported by a retaining means 150 such as table top, floor, lab bench or other suitable means to provide a substantially air tight seal between the hollow enclosure means and the retaining means.

[0100]FIG. 5 is a preferred embodiment of the invention in that the carrier gas is directed against the porous substrate and the trap and analysis means are substantially perpendicular to the initial flow of the carrier gas. Substantially perpendicular is understood to mean that the angle between the inlet means and the trap is between about 70 and about 110 degrees; preferably about 90 degrees.

[0101] The detailed description of the operation of the apparatus of FIG. 3A is set forth in the description of Example I, infra.

[0102] Thus, the following examples are illustrative of my invention, but my invention is only limited by the scope of the claims following said examples.

EXAMPLE 1 Analysis of Contents of Fragrance Composition Releasably Adhered to Towel

[0103] Objective:

[0104] To analyze the contents of a fragrance material originally situated in the interstices of a cotton towel.

[0105] Procedure:

[0106] A 4″×5.25″ cotton towel section containing 0.005% by weight fragrance composition is tightly wrapped around the central section of the inner enclosure of the apparatus of FIG. 3A. The inner enclosure thereof is composed of a porous fritted glass. Air from location 11 (FIG. 1B) is passed through the apparatus at a rate of 40 ml per minute for a period of 7 hours. Trapping means 22 contains a TENAX®-GC trap. At the end of the 7-hour period, the air flow was terminated and the TENAX®-GC trap was opened and the contents analyzed. The contents of the trap were analyzed by GC-MS analysis using a 50 m×0.32 mm OV-2 fused silica column having conditions: 80-220° C. at 8° C. per minute.

[0107]FIG. 4 is the GC mass spectrum for the perfume composition located on the towel, which is the subject of this example.

EXAMPLE 2

[0108] A towel having the dimensions of approximately 4 inches by approximately 5 inches, containing 0.005 weight percent fragrance is attached to the structure described in FIG. 5. Two trials were conducted, one trial was conducted were the towel remained stationary. In the second trial, the shaft was rotated at an speed of 82 revolutions per minute. In both trials the inert gas was provided to the enclosure means at a volume of 0.5 liters per minute. A chromatographic analysis of the headspace of the enclosure means was conducted.

[0109]FIG. 6A indicates the peaks found when the chromatographic analysis is performed while the towel was held stationary. FIG. 6B is the chromatographic analysis while the towel was rotated. As is evident from the chromatographic in FIG. 6B, the amount of material detected as much larger. In addition, there was a slight shifting of some of the peaks.

EXAMPLE 3

[0110] Two different commercially available fragrances were applied to a towel having the dimensions of Example 2 at a level of 0.005 weight percent. Using the apparatus described in FIG. 5, both fragrances were tested via while stationary and when rotated at a speed of 82 revolutions per minute. In all tests, the inert gas carrier was supplied to the hollow enclosure means at a rate of about 0.5 liters per minute.

[0111]FIG. 7 demonstrates the increase in volatile compounds detected from both fragrances when rotated compared to the stationary test. 

What is claimed is:
 1. Apparatus for quantitatively and qualitatively analyzing a volatile substance releasably bonded to a substantially planar pliable porous substrate having an inner surface and an outer surface, said substrate being porous to the passage of a carrier gas therethrough in a direction substantially perpendicular to the inner and outer surfaces of said planar pliable porous substrate comprising: (a) hollow enclosure means having: (i) hollow outer enclosure means comprising a hollow outer enclosure means first void space and, surrounding said outer enclosure means first void space, an outer gas-impermeable enclosure means wall having exit port means therethrough and entirely surrounding inner enclosure means, whereby a second void space exists having volume V₂ within said outer enclosure means and without said inner enclosure means; and (ii) inner enclosure means located entirely within said outer enclosure means first void space comprising an inner enclosure means third void space having volume V₁ and having two spaced-apart oppositely situated end sections and a central section juxtaposed to and communicating with each of said oppositely-situated end sections, said central section consisting essentially of support means having a substantially gas-permeable outer geometric laminar surface with at least one laminar gas-permeable section for both (A) supporting the pliable porous substrate whereby, when in use, said porous substrate covers said laminar gas-permeable section of said central section in an all encompassing manner and (B) enabling carrier gas to flow from within said inner enclosure means third void space to the second void space within said outer enclosure and without said inner enclosure, in a direction substantially perpendicular to and through said porous substrate, each of the two end sections being impervious to the flow of gas therethrough and one of said end sections having an entry port means communicating from without said hollow outer enclosure means to the first void space within said inner enclosure means; (b) analytical apparatus means located downstream from said hollow enclosure means and communicating with the exit port means thereof, comprising tube trapping means whereby volatile substance molecules emitted from said pliable porous substrate during gas flow therethrough are entrapped in said tube trapping means; and (c) upstream from said hollow enclosure means or downstream from said analytical apparatus means, inert gas flow effecting means for effecting the flow of inert gas sequentially (I) through said entry port means; (II) through porous pliable substrate means located on said support means; (III) through said exit port means; and (IV) through said analytical apparatus means.
 2. A process for quantitatively and qualitatively analyzing a volatile substance releasably bonded to a substantially planar pliable porous substrate having an inner surface and an outer surface comprising the steps of: (a) providing the apparatus of claim 1 ; (b) providing said porous substrate; (c) juxtaposing in an all encompassing manner said porous substrate with said support means of said central section of said inner enclosure means of said apparatus whereby the inner surface of said porous substrate is removably adhered to and intimately adjacent to the entirety of the laminar gas-permeable section of the outer geometric laminar surface of the support means; (d) effecting the flow of carrier gas sequentially (I) from a location upstream from the entry port means; (II) into the inner enclosure means; (III) past said support means through said entry port means; (IV) through said porous substrate means in a direction substantially perpendicular thereto in a substantially evenly distributed manner across the inner and outer surface thereof; (V) into and through said second void space; (VI) through said exit port means of said hollow outer enclosure means and into and through said analytical apparatus means; and (VII) whereby volatile substance molecules emitted from said porous substrate are trapped in said analytical apparatus means; and (e) employing the analytical apparatus means whereby analysis of the volatile molecules is effected.
 3. The apparatus of claim 1 wherein the central section of the inner enclosure means comprises porous glass frit.
 4. The apparatus of claim 1 wherein carrier gas filtering means is immediately upstream from said entry port of said inner enclosure means.
 5. The apparatus of claim 1 wherein carrier gas flow is effected by means of positive pressure from a source upstream from said inner enclosure means.
 6. The apparatus of claim 1 wherein carrier gas flow is effected into the inner enclosure means by means of negative pressure means downstream from said trapping means.
 7. The apparatus of claim 1 wherein the analytical apparatus means comprises a tube containing TENAX® trapping material.
 8. The apparatus of claim 1 wherein the analytical apparatus means comprises a solid phase microextraction means.
 9. The process of claim 2 wherein in step (e) a TENAX® trap is used and molecules extracted from the TENAX® trap are analyzed by means of NMR and IR analyses.
 10. The process of claim 2 wherein in step (e) solid phase microextraction is used, and the molecules obtained from the solid phase microextraction procedure are analyzed by means of NMR and IR analyses.
 11. The process of claim 9 wherein the pliable porous substrate is a cotton towel having fragrance molecules located thereon.
 12. The process of claim 10 wherein the pliable porous substrate used is a towel having fragrance molecules located thereon.
 13. The process of claim 11 wherein the carrier gas used is air.
 14. The process of claim 12 wherein the carrier gas used is air.
 15. The apparatus of claim 1 wherein the outer enclosure means and the inner enclosure means are in the shape of cylinders.
 16. Apparatus for quantitatively and qualitatively analyzing a volatile substance releasably bonded to a substantially planar pliable porous substrate having an inner surface and an outer surface, said substrate being porous to the passage of a carrier gas comprising: (a) hollow enclosure means supported by a retaining means thereby creating a hollow enclosure void space and, having exit port means therethrough; (b) analytical apparatus means located downstream from said hollow enclosure means and communicating with the exit port means thereof, comprising trapping means whereby volatile substance molecules emitted from said pliable porous substrate during gas flow therethrough are entrapped in said tube trapping means; and (c) upstream from said hollow enclosure means or downstream from said analytical apparatus means, inert gas flow effecting means for effecting the flow of inert gas sequentially (I) through said entry port means; (II) through porous pliable substrate means located on said support means; (III) through said exit port means; and (IV) through said analytical apparatus means; (d) means for moving the retaining means; and (e) means for attaching a porous pliable substrate means to the retaining means.
 17. A process for quantitatively and qualitatively analyzing a volatile substance releasably bonded to a substantially planar pliable porous substrate having an inner surface and an outer surface comprising the steps of: (a) providing the apparatus of claim 16 ; (b) providing said porous substrate; (c) moving said porous substrate with said support means; (d) effecting the flow of carrier gas sequentially (I) from a location upstream from the entry port means; (II) into the hollow enclosure means; (III) in proximity of said porous substrate means; (IV) through said exit port means of said hollow outer enclosure means and into and through said analytical apparatus means; and (V) whereby volatile substance molecules emitted from said porous substrate are trapped in said analytical apparatus means; and (e) employing the analytical apparatus means whereby analysis of the volatile molecules is effected.
 18. The method of claim 17 wherein the flow of the carrier gas is directed perpendicular to the motion of the porous carrier substrate.
 19. The method of claim 17 wherein the porous substrate motion is rotational.
 20. The method of claim 19 wherein the volatile substance molecules are emitted substantially perpendicular to the direction of the carrier gas as it enters the hollow enclosure means. 